Tetrafluoroethylene → Ethanesulfonic acid, 1,1,2,2-tetrafluoro-, sodium salt (1:1)
Reaction equation
[S:1]([O-:4])([O-:3])=[O:2].[Na+:5].[Na+].[F:7][C:8]([F:12])=[C:9]([F:11])[F:10]>O>[F:7][CH:8]([F:12])[C:9]([F:11])([F:10])[S:1]([O-:4])(=[O:3])=[O:2].[Na+:5]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 120 °C
Procedure
The sodium sulphite (201 g) was dissolved in water (600 mL) and taken in a 1000 mL Hastelloy reactor. Tetrafluoroethylene (150 g) was added to the reactor at −130° C. The temperature of the reactor was increased to 120° C. and maintained at 120° C. for 12 hours. The reactor was cooled to 25° C. and unreacted tetrafluoroethylene was vented off. The water of the reaction was removed from reaction mixture by azeotropic distillation to obtain a reaction mass. The reaction mass was extracted with hot ethanol using soxhlet apparatus. The ethanolic solution was concentrated to obtain pure sodium tetrafluoroethane sulfonate (100 g).
Workup
- customtaken in a 1000 mL Hastelloy reactor
- temperaturemaintained at 120° C. for 12 hours
- temperatureThe reactor was cooled to 25° C.
- customThe water of the reaction was removed from reaction mixture by azeotropic distillation
- customto obtain a reaction mass
- extractionThe reaction mass was extracted with hot ethanol using soxhlet apparatus
- concentrationThe ethanolic solution was concentrated
Sources & evidence
- ORD record
- ord-429142376b494d088084b38f5ed80ddc
- Source dataset
- uspto-grants-2016_06
- Patent number
- US09376379B2
Reaction notes
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